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(6Z)-6-[(1-methylpropyl)amino]methylidenecyclohexa-2,4-dien-1-one is a chemical compound classified under the group of organic compounds known as quinones. It is characterized by its yellow crystalline solid appearance and has a molecular formula of C13H19NO, with a molecular weight of 205.3 g/mol. (6Z)-6-[(1-methylpropyl)amino]methylidenecyclohexa-2,4-dien-1-one is predominantly utilized in the realm of chemical research and is not typically found in commercial products. Due to its potential health hazards, it is crucial to handle (6Z)-6-[(1-methylpropyl)amino]methylidenecyclohexa-2,4-dien-1-one with caution and to implement safety measures when working with this chemical.

5482-06-4

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5482-06-4 Usage

Uses

Used in Chemical Research:
(6Z)-6-[(1-methylpropyl)amino]methylidenecyclohexa-2,4-dien-1-one is used as a research compound for [application reason] in the field of chemical research. Its unique structure and properties make it a valuable tool for studying various chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 5482-06-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5482-06:
(6*5)+(5*4)+(4*8)+(3*2)+(2*0)+(1*6)=94
94 % 10 = 4
So 5482-06-4 is a valid CAS Registry Number.

5482-06-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (6Z)-6-[(butan-2-ylamino)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names N-sec-Butylsalicylideneamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5482-06-4 SDS

5482-06-4Downstream Products

5482-06-4Relevant academic research and scientific papers

Buttressing Salicylaldehydes: A Multipurpose Directing Group for C(sp3)?H Bond Activation

Yada, Akira,Liao, Wenqing,Sato, Yuta,Murakami, Masahiro

supporting information, p. 1073 - 1076 (2017/01/18)

A palladium-catalyzed reaction of primary amines with iodoarenes produces γ-arylated primary amines. A bulky salicylaldehyde, which is marked as easily available, installable, removable, and recoverable, plays a key role in directing palladium to site-selectively activate the C?H bond located γ to the amino group.

The Electrochemical Synthesis of Neutral Zinc(II) Complexes of Schiff Base Ligands: The Crystal Structure of Biszinc(II)

Sogo, T.,Romero, J.,Sousa, A.,Blas, A. de,Duran, M. L.,Castellano, E. E.

, p. 611 - 615 (2007/10/02)

The electrochemical synthesis and physico-chemical properties of neutral zinc(II) complexes of bidentate Schiff bases derived from salicylaldehydes are presented together with the X-ray structure of biszinc(II).The crystal is monoclinic, a = 21.877(3), b = 8.801(2), c = 12.027(5) Angstroem, β = 96.55(3) deg, space group C2/c.The complex is a monomer, and the zinc atom is tetrahedrally coordinated. - Keywords: X-Ray, Zinc, Schiff Bases, Electrochemical Synthesis

Synthesis and Reactions of Phenolic Alkylbenzylnitrosamines

Bowman, Peter J.,Brown, Ben R.,Chapman, M. Andrew,Doyle, Paul M.

, p. 701 - 770 (2007/10/02)

N-Alkyl-p-hydroxybenzylnitrosamines have been synthesised from p-benzoyloxybenzaldehydes via imines and amines which were nitrosated before removal of the protecting group with n-propylamine.N-Alkyl-o-hydroxybenzylnitrosamines were similarly obtained from o-methoxymethoxybenzaldehydes, the final deprotection being achieved with dilute acid.The nitrosamines decompose in hot aqueous alkali by two mechanisms, one through a quinone methide to yield a benzyl alcohol and the other by an elimination eventually yielding a benzaldehyde.The decomposition of the nitrosamines in the presence of 2-naphthol in alkaline solution results in alkylation of the naphthol and production of compounds from the reaction of 2-naphthol with the intermediate quinone methides.The N-sec-butylnitrosamines alkylate 2-naphthol on carbon but the N-methylnitrosamines alkylate on oxygen and during the methylation 94percent of deuterium exchange with methyl hydrogen occurs in deuterium oxide and there is 6percent intact transfer of the methyl group from the N-methylnitrosamine to the 2-naphthol.

N-Substituted Salicylaldimines Derivatives of Germanium(IV)

Singh, R. V.,Tandon, J. P.

, p. 1391 - 1398 (2007/10/02)

Hexa-coordinated Schiff base complexes of germanium of the general type Ge(OC2H5)2(SB)2 (SB(-) is the anion of the monofunctional bidentate Schiff base, SBH) have been synthesized by the reaction between ethyl-orthogermanate and the Schiff base in benzene

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